From Review to Launch
5 Steps to More Confident Supplement Launches
Step 1
Select your target markets and product
Set the countries in scope and enter the product description for review.
Step 2
Build the formula
Compile ingredients and dosage levels in one place for assessment.
Step 3
Compare markets side by side
See how ingredient rules, claims and warnings vary by country.
Step 4
Validate compliance and create labels
Use the results to prepare labels with more clarity and confidence.
Step 5
Maintain continuous compliance
Track regulatory changes over time as requirements evolve across markets.
Less manual work, more confident compliance
Make faster, more confident decisions with formula review, market comparison and labeling in Supplements Compliance
How We Help
Benefits of Supplements Compliance
Formula review in one place
Assess ingredients and dosage levels in one workflow
Bypass formula reviewing across scattered files and tools
Side by side country requirements comparison
See market differences clearly before moving forward
Avoid manual country-by-country checks that slow decisions
Market-by-market claims review
Check which claims fit each market more confidently
Avoid repeated claim checks for every market.
Compliant label creation
Turn compliance results into labels more quickly.
Eliminate manual labeling steps that create rework.
Regulatory change tracking
Stay current as requirements evolve across markets.
Never miss changes that affect products already in market.
End-to-end compliance management
Work in one place from review through labeling
No more switching between tools to complete one review
Extend Your Capabilities
Regulatory and R&D teams Extend Supplements Compliance with these Solutions
Pair Supplements Compliance with scientific insight and expert guidance to support product decisions, market entry and more complex regulatory needs.
FAQ
Supplement Compliance is a centralized Portfolio Compliance management system for every stage of development. It allows product development and regulatory teams to validate pre-launch, scale in multiple markets in parallel, and check European Union opportunities to expand business in the future. The result is faster market entry, reduced regulatory risk and greater confidence in your expansion strategy. This can be especially valuable for organizations preparing products for European markets.
The platform delivers a comprehensive and structured assessment, including:
• Full composition analysis with dashboard overview and detailed breakdown
• Claims guidance aligned with local EU regulations
• Required warnings and labeling elements
• Ready-to-use label outputs to accelerate market readiness
Supplements Compliance replaces fragmented manual checks with a single, streamlined workflow. This can also support activities related to food certifications and claims.
A user of Supplements Compliance can set up push notification alerts every time a supplement product is at risk due to an EU regulatory change. Organizations managing complex regulatory obligations may also benefit from regulatory and scientific affairs consulting.
Supplements Compliance software looks at European Union regulatory requirements for dietary supplements, including ingredients, labeling and claims. It directly impacts supplement formulation by ensuring only approved ingredients and dosages are used, which is essential for successful product approval and market access. Companies may also complement these activities with supplements consulting services to address formulation and regulatory challenges.
Common supplements compliance issues include the use of restricted or non-compliant ingredients, incorrect dosages in supplement formulation, misleading or unapproved claims on labels, and missing or incorrect information in supplements packaging. These issues can lead to regulatory delays, product rejections or recalls. Effective compliance management can also support product and label certification requirements as products move toward commercialization.